0132-0081 : Pedia-lax 1 g/1 Rectal Suppository
NDC: | 0132-0081 |
Labeler: | C.b. Fleet Company, Inc. |
Product Type: | Human OTC Drug |
Drug Name: | Pedia-lax |
Dosage Form: | Rectal Suppository |
Application #: | part334 |
Rev. Date: |
NDC Package Codes:
- 0132-0081-12: 12 SUPPOSITORY IN 1 JAR (0132‑0081‑12)
Active Ingredients:
- Glycerin
Dosage Strength:
- 1 g/1
Pharmaceutical Classes:
- Allergens [CS]
- Cell-mediated Immunity [PE]
- Glycerol [CS]
- Increased Histamine Release [PE]
- Increased IgG Production [PE]
- Non-Standardized Chemical Allergen [EPC]
Related Products:
Based on records with the same trade name.- 0132-0106 Pedia-lax 50 mg/118ml Oral Liquid by C.b. Fleet Company, Inc.
- 0132-0107 Pedia-lax 50 mg/15ml Oral Liquid by C.b. Fleet Company, Inc.
- 0132-0190 Pedia-lax 2.8 g/1 Rectal Liquid by C.b. Fleet Company, Inc.
- 0132-0195 Pedia-lax 2.8 g/4ml Rectal Liquid by C.b. Fleet Company, Inc.
- 0132-0202 Pedia-lax Rectal Enema by C.b. Fleet Company, Inc.
- 0132-0655 Pedia-lax Chewable 400 mg Chewable Tablet by C.b. Fleet Company, Inc.
NDC QR Code
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.